Method for preparing technetium-labeled antimony sulfide nanocolloid

ABSTRACT

The present invention relates to a preparation method for technetium-antimony sulfide nanocolloid, more precisely, a preparation method for technetium-antimony sulfide nanocolloid which is characterized by the processes of mixing and stirring of pertechnetate and antimony sulfide nanocolloid in the presence of borohydride exchange resin and obtaining technetium-antimony sulfide nanocolloid radioactive complex by irradiating microwave. The preparation of technetium-antimony sulfide nanocolloid complex in the present invention has advantages of obtaining technetium with high yield by inducing reaction at room temperature with borohydride exchange resin as a reducing agent and omitting a stage of pH re-adjusting, which has been generally required by the conventional method. In addition, a reducing agent is used as a solid phase instead of liquid solution, indicating that no matter how much a reducing agent is used, the reducing agent can be eliminated after reaction simply by filtering. Further, reaction time can be shortened by using microwave during the reaction, resulting in the shortening of preparation period for administration. So, the method of the present invention is economical and provides ready availability and shortened preparation time.

TECHNICAL FIELD

The present invention relates to a preparation method of technetium-antimony sulfide nanocolloid, more precisely, a preparation method of technetium-antimony sulfide nanocolloid using borohydride exchange resin (BER).

BACKGROUND ART

Technetium-99m (^(99m)Tc) is a kind of radionuclides which has been most widely used in diagnostic radiopharmaceuticals owing to its comparatively short half-life (6 hour) and gamma ray emission of 140 keV which is appropriate for obtaining a gamma image along with low prices and ready availability. The ^(99m)Tc forms a complex by working with a compound having a lone electron pair such as isocyanate group, amine group, carboxyl group, thiol group, etc, which is used as an imaging agent or a rebelling agent for various organs or tissues including lung, liver, brain, etc.

Reduction of technetium has to be performed prior to the reaction of pertechnetate and ligand to form a radioactive complex. At this time, reduction is performed by electrolysis or in general a reducing agent such as stannous chloride dihydrate, Fe⁺⁺, ascorbate containing Fe⁺⁺, formamidinesulfate, sodium borohydride, etc is used. Among those reducing agents, stannous chloride dihydrate is most popular.

Among many ^(99m)Tc complexes, ^(99m)Tc-Sb₂S₃ nanocolloid (technetium-99m labeled antimony sulfide nanocolloid, ^(99m)Tc-ASC) has been widely used for lymphoscintigraphy or bone marrow scintigraphy.

The ^(99m)Tc-Sb₂S₃ nanocolloid is formed by the reaction of pertechnetate and Sb₂S₃ nanocolloid in the presence of a reducing agent. As a reducing agent, SnCl₂, NaBH₄ or HCl can be used and actually HCl is preferred. SnCl₂ is the most popular reducing agent but has a problem of producing tin colloid during the preparation processes of nanocolloid. In the mean time, NaBH₄ has a problem of stability that is easily dropt by the variation of pH.

The ^(99m)Tc-Sb₂S₃ nanocolloid has been prepared by the conventional method as follows. Freeze-dried Sb₂S₃ nanocolloid and Na^(99m)TcO₄ are mixed together in the presence of HCl, followed by heating for 30 minutes. Then, a buffer is added and pH is adjusted to 6-7. The size of the obtained ^(99m)Tc-Sb₂S₃ nanocolloid particle is 5-20 nm (mostly 7-15 nm).

As explained above, the conventional preparation method for ^(99m)Tc-Sb₂S₃ nanocolloid requires HCl as a reducing agent, and at this time, it has to be heated for reaction. Such reaction at high temperature brings difficulties in handling and often causes break of chemical bond. Besides, pH has to be re-adjusted to neutral for the administration to a patient.

[Disclosure]

[Technical Problem]

It is an object of the present invention to provide an easier and much economical preparation method for technetium-antimony sulfide nanocolloid than the conventional method, in order to overcome the above problems, which is characterized by reaction at room temperature, omission of pH regulating stage and shortening of reaction time.

[Technical Solution]

In order to achieve the above object, the present invention provides a preparation method of technetium-antimony sulfide nanocolloid complex using borohydride exchange resin.

Hereinafter, the present invention is described in detail.

The present invention provides a preparation method for technetium-antimony sulfide nanocolloid complex using borohydride exchange resin as a reducing agent, more precisely, a preparation method for technetium-antimony sulfide nanocolloid complex resulted from stirring of the mixture of pertechnetate and antimony sulfide nanocolloid in the presence of borohydride exchange resin.

The method of the present invention characteristically uses borohydride exchange resin as a reducing agent. The borohydride exchange resin is structured by the bond of borohydride ion (BH₄ ⁻) to macromolecule attached cation. NH₄ ⁺ is used as a cation suitable for the fixation of borohydride ion. Every anion exchange resin having NH₄ ⁺ (quaternary ammonium functionality) can be used as an exchange resin for the fixation of borohydride ion. Such exchange resin is easily obtainable and is examplified by polystylene, high density polyethylene, amberite, etc.

The borohydride exchange resin is very stable in either acidic or basic condition, so it is easily applied to biomolecules and also simply eliminated by filtering.

In the present invention, reaction is carried out at room temperature. Contrary to the conventional method for preparing technetium-antimony sulfide nanocolloid complex performed at 100° C. the reaction is induced at room temperature in the method of the invention, indicating that it can minimize problems such as troublesome operations at high temperature, instability of chemical bond, etc.

Pertechnetate of the present invention is formed by ^(99m)TcO₄ ⁻, more preferably by Na^(99m)TcO₄, and antimony sulfide nanocolloid is prepared by the conventional method widely used in this field.

The present invention also provides a preparation method for technetitum-antimony sulfide nanocolloid complex, in which the mixture of pertechnetate and antimony sulfide nanocolloid was irradiated by microwave in the presence of borohydride exchange resin.

The final product is prepared by using the same starting material as described in the above method, and microwave irradiation is additionally performed. Microwave irradiation shortens reaction time. Precisely, reaction is completed within 1-2 minutes by microwave irradiation, which used to take 30 minutes with the conventional method, meaning the preparation time for the administration to a patient is shortened.

There is no fixed order for addition in the method of the present invention. Either simultaneous injection of pertechnetate and antimony sulfide nanocolloid to borohydride exchange resin or sequential injection of the two is possible. As shown in FIG. 3, it is preferred for the clinical use that pertechnetate and antimony sulfide nanocolloid are added to vial containing borohydride exchange resin, followed by reaction at room temperature for a while, and then technetium-antimony sulfide nanocolloid complex is obtained by using a syringe.

DESCRIPTION OF DRAWINGS

FIG. 1 is a set of microphotograph showing TEM image of technetium-antimony sulfide (^(99m)Tc-Sb₂S₃) nanocolloid, in particular, (a) shows ^(99m)Tc-Sb₂S₃ nanocolloid prepared in comparative example 1, and (b) shows ^(99m)Tc-Sb₂S₃ nanocolloid prepared in example 1,

FIG. 2 is a graph showing the stability of technetium-antimony sulfide (^(99m)Tc-Sb₂S₃) nanocolloid of the present invention,

FIG. 3 is a schematic diagram showing an example of clinical application of the method of the present invention.

MODE FOR INVENTION

Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples.

However, it will be appreciated that those skilled in the art, on consideration of this disclosure, may make modifications and improvements within the spirit and scope of the present invention.

PREPARATIVE EXAMPLE 1 Preparation of Antimony Sulfide Nanocolloides (ASC, Sb₂S₃)

Hydrogen sulfide (H₂S) was added into 120 ml of distilled water that was cooled to 0^(˜)5° C., resulting in the preparation of saturated hydrogen sulfide solution. 10 ml of 3.5% polyvinylpyrrolidone (PVP-mw 40,000) was added into the saturated hydrogen sulfide solution. After stirring for 5 minutes, 20 ml of 1% antimony potassium tartrate was added, followed by further stirring for 5 minutes to give antimony sulfide nanocolloid (Sb₂S₃ nanocolloid). Hydrogen sulfide was eliminated by using nitrogen gas, and the elimination of hydrogen sulfide was confirmed by lead acetate paper. The solution was filtered by 0.22 μm membrane filter, then sterilized and stored in a C refrigerator.

EXAMPLE 1 Preparation of ^(99m)Tc-ASC by the Method of the Present Invention

1.5 ml of distilled water was added to the mixture of 1.2 mg of Sb₂S₃ nanocolloid, 5 mg of borohydride exchange resin and 1 ml of Na^(99m)TcO₄ (40^(˜)50 mCi). The obtained solution was stirred at room temperature for 30 minutes until the reaction was completed. The resultant ^(99m)Tc-Sb₂S₃ nanocolloid (^(99m)Tc-labeled antimony sulfide nanocolloid) had a particle size ranging from 5 to 20 m (mostly 7^(˜)15 nm) (see FIG. 1 b).

Yield of the obtained ^(99m)Tc-Sb₂S₃ nanocolloid was measured by ITLC (instant thin-layer chromatography). And the results are shown in Table 1. TABLE 1 Chromatography System Kinds of ^(99m)Tc Supporter Solvent Origin Solvent Front ITLC-silica Acetone 100% ^(99m)Tc—Sb₂S₃ 0% ^(99m)TcO₄ ⁻ gel ITLC-silica Saline 100% ^(99m)Tc—Sb₂S₃ 0% ^(99m)TcO₄ ⁻ gel

As shown in Table 1, there was no observation of a peak of the first reactant at solvent front, but a peak of ^(99m)Tc-Sb₂S₃ was observed at origin. The results indicate that the complex is formed by the method of the present invention with over 99% yield.

EXAMPLE 2 Preparation of ^(99m)Tc-ASC by the Method of the Present Invention

1.5 ml of distilled water was added to the mixture of 1.2 mg of Sb₂S₃ nanocolloid, 5 mg of borohydride exchange resin and 1 ml of Na^(99m)TcO₄ (40^(˜)50 mCi). The obtained solution was irradiated with microwave for 1-2 minutes until the reaction was completed. The resultant ^(99m)Tc-Sb₂S₃ nanocolloid (^(99m)Tc-labeled antimony sulfide nanocolloid) had a particle size ranging from 5 to 20 nm (mostly 7^(˜)15 nm) (FIG. 1 b).

Yield of the obtained ^(99m)Tc-Sb₂S₃ nanocolloid was measured by ITLC (instant thin-layer chromatography). And the results are shown in Table 2. TABLE 2 Chromatography System Kinds of ^(99m)Tc Supporter Solvent Origin Solvent front ITLC-silica Acetone 100% ^(99m)Tc—Sb₂S₃ 0% ^(99m)TcO₄ ⁻ gel ITLC-silica Saline 100% ^(99m)Tc—Sb₂S₃ 0% ^(99m)TcO₄ ⁻ gel

As shown in Table 2, there was no observation of a peak of the first reactant at solvent front, but a peak of ^(99m)Tc-Sb₂S₃ was observed at origin. The results indicate that the complex is formed by the method of the present invention with over 99% yield.

COMPARATIVE EXAMPLE 1 Preparation of ^(99m)Tc-ASC by the Conventional Method

1.5 ml of distilled water was added to the mixture of 1.2 mg of Sb₂S₃ nanocolloid, 0.2 ml of 0.5 N HCL and 1 ml of Na^(99m)TcO₄. The solution was heated at 100° C. for 30 minutes, and then cooled at room temperature. At that time, pH was 1.5^(˜)1.8. 0.5 ml of sodium acetate buffer (0.35 M, pH 8) was added to adjust pH to 6.5. The resultant ^(99m)Tc-Sb₂S₃ (^(99m)Tc-labeled antimony sulfide nanocolloid) had a particle size ranging from 5 to 20 nm (mostly 7^(˜)15 nm) (see FIG. 1 a).

EXPERIMENTAL EXAMPLE 1 Stability of ^(99m)Tc-Sb₂S₃ Nanocolloid of the Present Invention

In order to investigate the stability of ^(99m)Tc-Sb₂S₃ nanocolloid of the present invention, ^(99m)Tc-Sb₂S₃ nanocolloid solution, prepared in the example 1, was stored in closed vacuum vials, which were left at room temperature for 1, 2, 4, 6, 8, 12, 16, 20, and 24 hours, respectively. The results are shown in FIG. 2.

As shown in FIG. 2, over 98% stability was not changed until 24 hours.

INDUSTRIAL APPLICABILITY

As explained hereinbefore, contrary to the conventional preparation method, the preparation method for technetium-antimony sulfide nanocolloid complex of the present invention is characterized by using borohydride exchange resin as a reducing agent, inducing reaction at room temperature to give technetium complex with high yield and shortening reaction time by omitting pH re-adjusting process. In addition, the reduction is achieved not in liquid but in solid phase, so a reducing agent can be easily eliminated by simple filtering regardless of its used amount. Thus, the preparation of the complex by the method of the present invention is easier and much economical than the conventional method. Besides, reaction time is shortened by using microwave, meaning that preparation time for administration to a patient is much reduced.

Those skilled in the art will appreciate that the conceptions and specific embodiments disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims. 

1. A preparation method for technetitum-antimony sulfide nanocolloid complex, in which pertechnetate and antimony sulfide nanocolloid was mixed and stirred in the presence of borohydride exchange resin.
 2. A preparation method for technetitum-antimony sulfide nanocolloid complex, in which the mixture of pertechnetate and antimony sulfide nanocolloid was irradiated by microwave in the presence of borohydride exchange resin.
 3. The preparation method for technetium-antimony sulfide nanocolloid complex as set forth in claim 2, wherein the irradiation time of microwave is 1-2 minutes.
 4. The preparation method for technetium-antimony sulfide nanocolloid complex as set forth in claim 1 or claim 2, wherein the pertechnetate is Na^(99m)TcO₄.
 5. The preparation method for technetium-antimony sulfide nanocolloid complex as set forth in claim 1 or claim 2, wherein the method is carried out at room temperature.
 6. The preparation method for technetium-antimony sulfide nanocolloid complex as set forth in claim 1 or claim 2, wherein the resultant has a particle size ranging from 5 to 20 nm. 